| Literature DB >> 29958802 |
Marko Šestan1, Sonja Marinović1, Inga Kavazović1, Đurđica Cekinović2, Stephan Wueest3, Tamara Turk Wensveen4, Ilija Brizić5, Stipan Jonjić6, Daniel Konrad3, Felix M Wensveen1, Bojan Polić7.
Abstract
Pro-inflammatory cytokines of a T helper-1-signature are known to promote insulin resistance (IR) in obesity, but the physiological role of this mechanism is unclear. It is also unknown whether and how viral infection induces loss of glycemic control in subjects at risk for developing diabetes mellitus type 2 (DM2). We have found in mice and humans that viral infection caused short-term systemic IR. Virally-induced interferon-γ (IFN-γ) directly targeted skeletal muscle to downregulate the insulin receptor but did not cause loss of glycemic control because of a compensatory increase of insulin production. Hyperinsulinemia enhanced antiviral immunity through direct stimulation of CD8+ effector T cell function. In pre-diabetic mice with hepatic IR caused by diet-induced obesity, infection resulted in loss of glycemic control. Thus, upon pathogen encounter, the immune system transiently reduces insulin sensitivity of skeletal muscle to induce hyperinsulinemia and promote antiviral immunity, which derails to glucose intolerance in pre-diabetic obese subjects. VIDEO ABSTRACT.Entities:
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Year: 2018 PMID: 29958802 DOI: 10.1016/j.immuni.2018.05.005
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745